EP0893508A3 - Neues Verfahren zur Herstellung von Oxodicyclopentadien - Google Patents

Neues Verfahren zur Herstellung von Oxodicyclopentadien Download PDF

Info

Publication number
EP0893508A3
EP0893508A3 EP98250265A EP98250265A EP0893508A3 EP 0893508 A3 EP0893508 A3 EP 0893508A3 EP 98250265 A EP98250265 A EP 98250265A EP 98250265 A EP98250265 A EP 98250265A EP 0893508 A3 EP0893508 A3 EP 0893508A3
Authority
EP
European Patent Office
Prior art keywords
oxodicyclopentadiene
producing
new method
optically active
acetate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP98250265A
Other languages
English (en)
French (fr)
Other versions
EP0893508A2 (de
Inventor
Kunio Ogasawara
Takahiko Taniguchi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JNC Corp
Original Assignee
Chisso Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chisso Corp filed Critical Chisso Corp
Publication of EP0893508A2 publication Critical patent/EP0893508A2/de
Publication of EP0893508A3 publication Critical patent/EP0893508A3/de
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/004—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of alcohol- or thiol groups in the enantiomers or the inverse reaction
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P15/00—Preparation of compounds containing at least three condensed carbocyclic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
EP98250265A 1997-07-25 1998-07-21 Neues Verfahren zur Herstellung von Oxodicyclopentadien Withdrawn EP0893508A3 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP9213840A JPH1142095A (ja) 1997-07-25 1997-07-25 新規なオキソジシクロペンタジエンの製造方法
JP213840/97 1997-07-25

Publications (2)

Publication Number Publication Date
EP0893508A2 EP0893508A2 (de) 1999-01-27
EP0893508A3 true EP0893508A3 (de) 1999-03-03

Family

ID=16645903

Family Applications (1)

Application Number Title Priority Date Filing Date
EP98250265A Withdrawn EP0893508A3 (de) 1997-07-25 1998-07-21 Neues Verfahren zur Herstellung von Oxodicyclopentadien

Country Status (3)

Country Link
US (1) US5900369A (de)
EP (1) EP0893508A3 (de)
JP (1) JPH1142095A (de)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08336396A (ja) * 1995-06-12 1996-12-24 Chisso Corp 光学活性エンド−３−ヒドロキシジシクロペンタジエンの製造法
JPH09206093A (ja) * 1996-02-08 1997-08-12 Chisso Corp 光学活性ジシクロペンタジエン誘導体の製造法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2104306C1 (ru) * 1989-11-13 1998-02-10 Пфайзер Инк. Способ получения оптически активного (2s)- или (2r)-эндо-бицикло[2.2.1]гептан-2-ола, способ получения 5-(3-[(2r)-экзо-бицикло[2.2.1]гепт-2-илокси]-4-метоксифенил)-3,4,5,6-тетрагидропиримидин-2(1н)-она, оптически активный 5-(3-[экзо-бицикло[2.2.1]гепт-2-илокси]4-метоксифенил)-3,4,5,6-тетрагидропиримидин-2(1н)-он, оптически активные промежуточные соединения и способ их получения
US5374768A (en) * 1992-08-19 1994-12-20 Chisso Corporation Cyclohexene derivatives
JPH06335398A (ja) * 1993-05-31 1994-12-06 Chisso Corp シクロヘキセンジオール誘導体
JP3638643B2 (ja) * 1994-10-14 2005-04-13 高砂香料工業株式会社 光学活性１−オクテン−３−オールの製造法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08336396A (ja) * 1995-06-12 1996-12-24 Chisso Corp 光学活性エンド−３−ヒドロキシジシクロペンタジエンの製造法
JPH09206093A (ja) * 1996-02-08 1997-08-12 Chisso Corp 光学活性ジシクロペンタジエン誘導体の製造法

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
B. M. TROST ET AL.: "Stereocontrolled Approach to 1,4-Disubstituted 1,3-Dienes", J. ORG. CHEM., vol. 43, no. 24, 1978, pages 4559 - 4564, XP002087928 *
CHEM. COMMUN., vol. 15, 1997, CAMBRIDGE, pages 1399 - 1400 *
CHEMICAL ABSTRACTS, vol. 126, no. 12, 24 March 1997, Columbus, Ohio, US; abstract no. 156486, OGASAWARA, KUNIRO: "Optically active endo-3- hydroxydicyclopentadiene manufacture with lipase" XP002087930 *
CHEMICAL ABSTRACTS, vol. 127, no. 18, 3 November 1997, Columbus, Ohio, US; abstract no. 247194, OGASAWARA, KUNIRO: "Manufacture of optically active dicyclopentadienes with lipase" XP002087931 *
CHEMICAL ABSTRACTS, vol. 127, no. 20, 17 November 1997, Columbus, Ohio, US; abstract no. 278001, TANIGUCHI, TAKAHIKO ET AL: "Lipase-triethylamine-mediated dynamic transesterification of a tricyclic acyloin having a latent meso-structure: a new route to optically pure oxodicyclopentadiene" XP002087929 *
T. TANIGUCHI AND K. OGASAWARA: "Asymmetrization of a Meso 1,2-Enediol Bis(trimethylsilyl) Ether using a (S)-Binol Monoisipropyl Ether(BINOL-Pr)-Tin Tetrachloride Complex.", TETRAHEDRON LETT., vol. 38, no. 36, 1997, pages 6429 - 6432, XP004087956 *
T. TANIGUCHI ET AL.: "Lipase-mediated kinetic resolution of tricyclic acyloins.", TETRAHEDRON: ASYMMETRY, vol. 8, no. 16, 1997, pages 2773 - 2780, XP004090363 *

Also Published As

Publication number Publication date
JPH1142095A (ja) 1999-02-16
US5900369A (en) 1999-05-04
EP0893508A2 (de) 1999-01-27

Similar Documents

Publication Publication Date Title
EP0382173A3 (de) Substanz PF 1022, Verfahren zu ihrer Herstellung und diese Substanz enthaltende anthelmintische Zusammensetzung
DE69434590D1 (de) Maltose-Trehalose-konvertierendes Enzym, dessen Herstellung und Verwendung
PL322611A1 (en) Methods of obtaining l-amini acid by fermentation, dna as well as micro-organism
EP0821058A3 (de) Verfahren zur Erhöhung der Enzym-Aktivität bei erhöhter Temperatur
AU5619999A (en) Method for reacting an organic compound with a hydroperoxide
IL145288A (en) Isolated cytokine zalpha11 ligand polypeptide and uses thereof
EP0827965A3 (de) Synthese von 9-Deoxo-9a-Aza 11,12-Deoxy-9a-Methyl-9a-Homoerythromycin A 11,12-hydrogenorthoborat-dihydrat
DE60028777D1 (de) Verfahren zur herstellung von 1,3-propanediol durch einen rekombinanten micro-organismus in abwesenheit von coenzym b12
AU5961596A (en) Method for expression and isolation of biologically active m olecules in urine
EP0816880A3 (de) Verfahren zur Herstellung eines optischen Wellenleitersubstrats
EP0733709A3 (de) Mutierte Farnesyldiphosphatesynthase befähigt zum Synthetisieren von Geranylgeranyldiphosphat und dafür kodierende Gene
ATE240924T1 (de) Verfahren zur herstellung von methylmercatopropanal
EP0849306A3 (de) Methode zur Kontrolle der effektiven Katalysatormenge bei der Darstellung von Polycarbonat durch Umesterung
EP0882739A3 (de) Polymer mit hohen molekular Gewicht und Verfahren zu seiner Herstellung und Reibungsreduzierendes Mittel
EP1308453A3 (de) Verfahren zur Herstellung von Platin Verbindungen
EP0893508A3 (de) Neues Verfahren zur Herstellung von Oxodicyclopentadien
EP0361304A3 (de) Verfahren zur Herstellung von Alkadienolen
CA2018562A1 (en) Process for the enzymatic cleavage of vinyl 2-aryl-propionates
EP0298756A3 (de) Optisch aktive Allylalkohol und Verfahren zur Herstellung von Leucotrien-B4, das sie verwendet
EP0606485A4 (de) Verfahren zur herstellung einer substanz zur senkung des cholesterinspiegels.
ES8700652A1 (es) Un metodo de preparar n-4-(3-aminopropil)-aminobutil-2,2-di-hidroxietanoamida
EP0801070A3 (de) Verfahren zur Herstellung von Platin Verbindungen
EP0391345A3 (de) Verfahren zur Herstellung optisch aktiver Substanzen
MY126497A (en) Method for producing hydrolyzed protein.
AU7265087A (en) Animal cell transformant, method for obtaining the transformant and method for producing desired foreign gene product by using the transformant

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): CH DE FR GB LI

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

17P Request for examination filed

Effective date: 19990903

AKX Designation fees paid

Free format text: CH DE FR GB LI

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20030201